Pilot Study on Auricular Acupuncture (at the Ear Level) in Hospitalized Adults with Borderline Personality Disorder
Résumé de l'étude
This study aims to evaluate an auricular acupuncture program (at the ear level), conducted by nurses, as a complement to usual care, in hospitalized adults in psychiatry for borderline personality disorder. The intervention is based on a standardized protocol from the National Acupuncture Detoxification Association (NADA), also known as "acudetox". Acupuncture is performed by mental health nurses trained as NADA practitioners. In this pilot study, we will recruit 15 patients. The objective is to assess the feasibility of the program in terms of participation in the sessions, as well as its potential impact on several aspects of health, particularly: emotion regulation, relaxation, sleep quality, satisfaction with treatments, clinical severity and evolution, and the use of psychotropic medications. Participation in the study is voluntary and lasts 12 days. Individuals who agree to participate will be invited to: - attend 5 scheduled acupuncture sessions between 4:00 PM and 8:00 PM, spaced 24 hours apart; - have a follow-up visit 2 days after the end of the program; - complete short questionnaires between sessions. All participants will receive acupuncture in addition to the usual care provided by the psychiatric hospital. This care includes medical consultations, medication treatments, as well as support from nurses, physiotherapists, occupational therapists, and social workers. The results of this pilot study will provide essential information on research procedures as well as any necessary adaptations before considering a larger-scale study. Each participant will receive a shopping voucher (20 CHF Migros) at the end of each visit, for a total maximum amount of 120 CHF.
(BASEC)
Intervention étudiée
The intervention protocol consists of a short and standardized auricular acupuncture program, administered during psychiatric hospitalization. Participants will receive 5 individual acupuncture sessions (45 minutes each) over a period of 9 days, scheduled at 24-hour intervals and conducted between 4:00 PM and 8:00 PM. Each session will take place in the patient's hospital room and will be performed by a mental health nurse trained as a NADA practitioner.
After a brief explanation of the procedure, participants are comfortably positioned either semi-sitting or lying down. The nurse then prepares the auricular area according to standard hygiene procedures, and inserts sterile single-use needles bilaterally (in both ears) at the five points specified by the NADA protocol. The insertion of the needles lasts about 15 minutes and is performed with minimal verbal interactions, in accordance with the principles of the protocol. This is followed by a silent period of 30 minutes, during which the patient remains alone in a calm and uninterrupted environment. At the end of the session, the nurse removes the needles and conducts a clinical assessment of the skin condition (bleeding, bruising) and documents the procedure.
The intervention is not intended to be personalized or adapted at the individual level. All participants will receive the same standardized auricular acupuncture protocol as provided by NADA, applied uniformly during all sessions. Only minor adjustments may be made if necessary (e.g., slight adjustment of needle positioning in case of pain); these do not alter the therapeutic content and do not compromise the integrity of the intervention.
All operational adjustments will be documented as deviations from the protocol, specifying their nature and justification.
(BASEC)
Maladie en cours d'investigation
Borderline Personality Disorder
(BASEC)
The study concerns hospitalized adults with a diagnosis of borderline personality disorder, capable of expressing themselves and understanding French, regardless of the ongoing treatment provided at the hospital (psychotherapy, medications, etc.). (BASEC)
Critères d'exclusion
Patients presenting severe agitation, high suicide risk, those hospitalized in isolation rooms, or receiving anticoagulant or immunosuppressive treatment will be excluded from the study. (BASEC)
Lieu de l’étude
Lausanne
(BASEC)
Sponsor
Centre hospitalier universitaire vaudois (CHUV) - Bureau Promoteur de la recherche
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Jenny Gentizon, infirmière Ph.D
+41795568033
jenny.gentizon@clutterchuv.chInstitut Universitaire de Formation et Recherche en Soins, UNIL/CHUV
(BASEC)
Informations générales
University of Applied Sciences and Arts Western Switzerland
(ICTRP)
Informations scientifiques
University of Applied Sciences and Arts Western Switzerland
(ICTRP)
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Commission cantonale d'éthique du Vaud
(BASEC)
Date d'approbation du comité d'éthique
12.05.2026
(BASEC)
Identifiant de l'essai ICTRP
NCT05715190 (ICTRP)
Titre officiel (approuvé par le comité d'éthique)
Feasibility and preliminary effectiveness of a nurse-led auricular acupuncture intervention in hospitalized adults with borderline personality disorder: a pilot study (BASEC)
Titre académique
Development and Feasibility of a Nurse-led Person-centered Education Program on Percentage Reduction of Psoriasis in Persons With Psoriasis: a Pilot Study (ICTRP)
Titre public
Development and Feasibility of a Nurse-led Person-centered Education Program (ICTRP)
Maladie en cours d'investigation
Self-ManagementBehaviorPatient Empowerment (ICTRP)
Intervention étudiée
Other: Education (ICTRP)
Type d'essai
Interventional (ICTRP)
Plan de l'étude
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Health Services Research. Masking: None (Open Label). (ICTRP)
Critères d'inclusion/exclusion
Inclusion Criteria:
- Diagnosed cutaneous psoriasis, regardless of the stage of the disease and treatment
type (systemic and/or topic, and/or puva therapy)
- Age over 18 years
- Proficiency in the French language
Exclusion Criteria:
- Valid informed consent is not or cannot be given
- Patients unable to follow the 6-session therapeutic education program
- Patients currently engaged in any other therapeutic education program (ICTRP)
non disponible
Critères d'évaluation principaux et secondaires
percentage reduction of psoriasi (ICTRP)
Health Literacy;Patient benefit;Life Quality Index;Psoriasis severity;Medication knowledge;Knowledge of psoriasis;Self-management of the disease (ICTRP)
Date d'enregistrement
non disponible
Inclusion du premier participant
non disponible
Sponsors secondaires
University of Lausanne Hospitals;University of Lausanne (ICTRP)
Contacts supplémentaires
Sebastian E Probst, Prof, University of Applied Sciences and Arts Western Switzerland (ICTRP)
ID secondaires
Psoriasis (ICTRP)
Résultats-Données individuelles des participants
non disponible
Informations complémentaires sur l'essai
https://clinicaltrials.gov/study/NCT05715190 (ICTRP)
Résultats de l'essai
Résumé des résultats
non disponible
Lien vers les résultats dans le registre primaire
non disponible